CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Cytokine release syndrome and relevant factors of CD19 targeted chimeric antigen receptor T cell therapy in relapsed/refractory B cell hematological malignancies.
Cytokine release syndrome and relevant factors of CD19 targeted chimeric antigen receptor T cell therapy in relapsed/refractory B cell hematological malignancies.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
作为 CAR-T 治疗的常见不良反应,CRS 的严重程度可通过剂量递增输注减轻,移植史与较轻的 CRS 相关。
完全缓解(CR)率为 74.0%(57/77)。77 个疗程中有 68 个(88.3%)发生任何级别 CRS,1、2、3、4 和 5 级分别占 32.5%、24.7%、22.1%、6.5% 和 2.6%。有移植史的患者 CRS 较轻;基于剂量递增的输注可降低 CRS 严重程度。重度 CRS 与较高 CR 率相关,但对无事件生存期(EFS)、无复发生存期(RFS)或总生存期(OS)无显著影响。
CRS 是 CAR-T 治疗的常见不良反应,可通过剂量递增输注减轻其严重程度;移植史与较轻 CRS 相关。重度 CRS 与较好应答相关,但与长期生存无关。
The rate of complete remission (CR) was 74.0% (57/77). CRS of any grade occurred in 68 of 77 episodes (grade 1: 32.5%, grade 2: 24.7%, grade 3: 22.1%, grade 4: 6.5%, grade 5: 2.6%). Patients with a history of transplantation had less severe CRS, and dose escalation-based infusion reduced the severity of CRS. Severe CRS was related to a higher CR rate but had no significant impact on event-free survival (EFS), relapse-free survival (RFS), or overall survival (OS).
As a common adverse reaction of CAR-T therapy, the severity of CRS can be alleviated by dose escalation infusion, a history of transplantation was correlated with less severe CRS. Severe CRS was related to better response but was unrelated to long-term survival.
MEMBER ACCOUNT
登录成功会直接打开下一页。